Systems and methods for intramedullary nail implantation

ABSTRACT

Intramedullary nails, systems, and methods. The intramedullary nail may include a generally elongate body extending from a first, distal end to a second, proximal end. The distal end may include one or more openings configured to receive one or more bone anchors that extend transversely through the distal end intramedullary nail, and thereby configured to secure the distal end of the nail. The proximal end may also include one or more openings configured to receive one or more bone anchors that extend transversely through the proximal end of the intramedullary nail, and thereby configured to secure the proximal end of the nail. In some embodiments, the proximal end may further include a cross-locking feature, which includes a second bone anchor that interlocks with a first bone anchor, for example, for enhanced bone purchase and bony fixation.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation-in-part of U.S. patent applicationSer. No. 15/272,850, filed Sep. 22, 2016, which is incorporated byreference herein in its entirety for all purposes.

TECHNICAL FIELD

The present technology is generally related to intramedullary nailimplantation for treatment of bone fractures. In particular, severalembodiments are directed to systems and methods for implanting anintramedullary nail for immobilizing bone fractures.

BACKGROUND

The significant long bones of the extremities are the humerus, radiusand ulna of the upper extremity and the femur and tibia of the lowerextremity. Following an injury to the long bone, and in particular,injuries resulting in one or more fractures of the long bone, one ormore fixation devices may be used to immobilize the fracture fragmentsand stabilize the long bone. Bone fractures can be treated with screwsor other fixation devices inserted into or through the bone to stabilizeit once the fractured portions have been brought into proper alignment.Femoral neck fixation, for example, can be used to treat hip fracturesby inserting an intramedullary nail into the medullary cavity of thefractured femur followed by insertion of a fixation screw into thefemoral neck/head at an angle relative to the intramedullary nail.Similarly, other long bone fractures can be treated by inserting anintramedullary nail into the intramedullary canal of the bone andproviding the appropriate proximal and/or distal fixation. Traditionalintramedullary devices may suffer from a number of disadvantages,however. For example, they may be susceptible to implant failure anddifficulty in alignment of the fixation screw with respect to theintramedullary nail. Accordingly, there is a need for improved systemsand methods for intramedullary nail implantation.

SUMMARY

Intramedullary nails, systems, insertion tools, and method of treatmentare provided. The intramedullary nails may be suitable for implantingwithin a medullary canal of a fractured long bone and subsequentlyproviding proximal fixation and/or distal fixation, for example, withone or more anchors, fasteners, fixation screws, or the like. Suitablelong bones may include the humerus, radius, ulna, femur, tibia, or thelike. Although generally described with reference to the femur, it willbe appreciated that the intramedullary nail and system may be adaptedfor use with any long bone.

According to one aspect, an intramedullary nail is provided. Theintramedullary nail may comprise a generally elongate body extendingfrom a first, distal end to a second, proximal end. The distal end mayinclude one or more openings configured to receive one or more boneanchors or fasteners that extend transversely through the distal endintramedullary nail, and thereby configured to secure the distal end ofthe nail. The proximal end may also include one or more openingsconfigured to receive one or more bone anchors or fasteners that extendtransversely through the proximal end of the intramedullary nail, andthereby configured to secure the proximal end of the nail.

In one aspect, a system for inserting an intramedullary nail into a boneis provided. The system includes an intramedullary nail with an openingor aperture formed therein. An insertion tool includes can temporarilyengage with an end of the intramedullary nail during implantation, andrelease from the nail once the procedure is complete. A receivingfeature for a guide sheath (e.g., a hole, recess, etc.) is disposed inthe handle portion and can receive a guide sheath therethrough. Thereceiving feature defines an axis such that, when the intramedullarynail is coupled to the coupling portion, a guide sheath inserted throughthe receiving feature substantially aligns with the aperture in theintramedullary nail. A first retention member is disposed in theinsertion tool adjacent to the guide sheath receiving feature. The firstretention member can interact with a second retention member on theguide sheath to form a ratchet-like mechanism that restrict movement ofthe guide sheath with respect to the receiving feature. A retentionrelease mechanism can be located on a lower portion (e.g., a bottomsurface) of the insertion tool. A guide wire receptacle (e.g., a hole,recess, etc.) can receives a guide wire therethrough and is positionedsuch that, when the intramedullary nail is coupled to the couplingportion, a guide wire inserted through the receiving feature runs alongan axis adjacent to the side surface of the intramedullary nail.

In another aspect, a method for inserting an intramedullary nail into apatient is provided. The method includes inserting a nail into amedullary canal of a patient along a first axis. For insertion, the nailis coupled at its proximal end to an insertion tool. A guide wire isinserted through a guide wire hole in the insertion tool along a secondaxis such that the guide wire runs nearby or adjacent to a side surfaceof the nail. A screw or other bone fixation device is inserted throughreceptacle (e.g., a hole, recess, or other suitable structure) formed inthe insertion tool such that the screw passes through an aperture formedin the nail.

In accordance with another aspect, an implant is provided. The implantincludes an intramedullary nail that is elongated along a first axis.First and second openings or apertures are disposed in a proximalportion of the nail. The first aperture defines a second axis transverseto the first axis, and the second aperture defines a third axistransverse to the first axis. The third axis intersects with the secondaxis at a point spaced apart from the nail. In some embodiments, thefirst screw can be inserted through the first aperture along the secondaxis and a second screw can be inserted through the second aperturealong the third axis. The second screw can be at least partiallyinserted through a slot in the first screw such that the two screwsinterlock. The second screw can be shorter than the first screw but longenough that at least a threaded distal tip extends beyond the slot inthe first screw to provide some purchase in the bone.

In accordance with another embodiment, an implant includes anintramedullary nail, a first fixation device, and a second fixationdevice. The intramedullary nail has an elongate body extending from aproximal portion to a distal portion where a portion of the elongatebody extends along a first axis. A first aperture is formed in theproximal portion. The first aperture defines a second axis transverse tothe first axis. A second aperture is formed in the proximal portion. Thesecond aperture is spaced apart from the first aperture. The secondaperture defines a third axis transverse to the first axis. The thirdaxis intersects with the second axis at a point spaced apart from thebody. The first fixation device is positionable through the firstaperture in the nail. The first fixation device has an elongate slotextending therethrough. The second fixation device is positionablethrough the second aperture in the nail, and the second fixation deviceis positionable through the elongate slot in the first fixation device.

Also provided are kits including intramedullary nails of varying shapesand sizes, bone anchors, fasteners, insertion tools, and components forinstalling the same.

BRIEF DESCRIPTION OF THE DRAWINGS

A more complete understanding of the present invention, and theattendant advantages and features thereof, will be more readilyunderstood by reference to the following detailed description whenconsidered in conjunction with the accompanying drawings wherein:

FIGS. 1A and 1B illustrate a system for implanting an intramedullarynail.

FIGS. 2A-2C illustrate various views of an insertion handle of thesystem shown in FIGS. 1A and 1B.

FIGS. 3A-3F illustrate steps of implanting an intramedullary nail into afractured femur.

FIGS. 4A-4D illustrate various views of an intramedullary nail and afirst fixation device.

FIGS. 5A-5D illustrate various views of the first fixation deviceinserted through the intramedullary nail.

FIGS. 6A-6D illustrate various views of a second fixation device and theintramedullary nail with the first fixation device inserted therein.

FIGS. 7A-7D illustrate various views of the second anchor insertedthrough the intramedullary nail and the first fixation device.

FIGS. 8A-8C illustrate steps of implanting an intramedullary nail withinterlocking fixation devices into a fractured femur.

FIGS. 9A-9C depict various views of an intramedullary nail and a firstfixation device according to another embodiment.

FIGS. 10A-10C illustrate various views of the first fixation deviceinserted through the intramedullary nail.

FIGS. 11A-11C illustrate various views of a second fixation deviceinserted through the intramedullary nail and the first fixation device.

FIGS. 12A-12E illustrate various views of the second fixation deviceinserted through the intramedullary nail and the first fixation device.

DETAILED DESCRIPTION

Intramedullary nails, systems, insertion tools, and method of treatmentare provided. The intramedullary nails may be suitable for implantationwithin the intramedullary canal of a fractured long bone andsubsequently providing proximal fixation and/or distal fixation, forexample, with one or more anchors, fasteners, fixation screws, or thelike. Suitable long bones may include the humerus, radius, ulna, femur,tibia, or the like. Although further described with reference to hipfractures of the femur, it will be appreciated that the intramedullarynail and system may be adapted for use with any long bone.

In conventional hip fracture fixation techniques, there are four mainfailure modes: axial cutout, cephalad cutout, proximal fragmentrotation, and nonunion. “Cutout” is the term for hip screw subsidenceinto the articular surface of the hip. Cutout can occur in either acephalad (toward the head) or axial direction (along the axis of the hipscrew). Axial cutout is the result of an implant with a small axialprofile that provides little resistance to axial translation. Axialcutout can be addressed by the “controlled collapse” features on certainmodern hip fracture nails; the hip screw is allowed to translate throughthe nail, even after the set screw is locked in place. Cephalad cutoutis the radial translation of the nail which is the result of a narrowimplant that “windshield wipers” through the weak cancellous bone in thehip. Proximal fragment rotation is the result of a circular profile hipscrew that acts as a fulcrum to the proximal hip fragment. Fracturenonunion is the result of biologic or mechanical factors that areincompatible with the bone healing process. Biologic factors of thepatient are not controllable by the implant. Mechanical factors arethose that typically allow fixation that is too rigid or too flexible.Nonunion is usually the precursor to one of the other three failuremodes. Occasionally, nonunion will cause the nail to break in fatiguebefore the bone fails.

The intramedullary nails and systems described herein may address one ormore of these failure modes. In some embodiment, the intramedullary nailincludes proximal and distal locking, for example, to prevent cutout. Inother embodiments, the intramedullary nail may include proximal lockingincluding two interlocking fixation devices (e.g., screws), for example,by providing converging and diverging purchase, along with bony fixationin the calcar of the femur, which is the strongest portion of the hipbone. Accordingly, the risk of failure due to cutout and/or rotation canbe reduced.

Additionally, some intramedullary nail implantation systems fail toadequately address the problems of fragment rotation duringimplantation. Rotation occurs when fragments of the bone rotate aboutthe axis of the screw during the implantation procedure. Conventionalanti-rotation technologies require the use of additional instruments orare limited to a single wire placement. In some embodiments, aninsertion tool is directly coupled to the intramedullary nail andadditional instruments are not needed for the placement of ananti-rotation guide wire and allow the user to place one or more guidewires anterior and/or posterior to the nail. These guide wires can bepositioned to prevent the distal fragments of the femoral head and neckfrom rotating about the axis of the anchor during the procedure.

Some systems may be susceptible to backout during the implantationprocedure. Backout occurs when the guide sheath used to insert the screwthrough the intramedullary nail moves proximally away from the bone.Conventional systems either have no features to prevent backout or elseprovide backout prevention measures that obstruct the normal positioningof the hands during the procedure, resulting in the risk of releasingthe guide sheaths and dropping them to the floor. Ratchets on theinsertion tool may have the release button facing towards the gripportion on the insertion tool and may present the danger of the user'shand slipping and inadvertently pressing the button. Accidentallypressing the button could result in releasing the sheath and causing thesheath to fall on the floor. In some embodiments, a backout preventionsystem (e.g., a ratchet system) may be disposed on the lower end of theinsertion tool, which allows a user to have a hand placed on the grip ofthe insertion tool without the risk of inadvertently pressing theratchet release button.

Further specific details of several embodiments of the presenttechnology are described below with reference to FIGS. 1A-8C. Althoughmany of the embodiments are described below with respect to devices,systems, and methods for implantation of intramedullary nails, otherembodiments are within the scope of the present technology.Additionally, other embodiments of the present technology can havedifferent configurations, components, and/or procedures than thosedescribed herein. For example, other embodiments can include additionalelements and features beyond those described herein, or otherembodiments may not include several of the elements and features shownand described herein.

For ease of reference, throughout this disclosure identical referencenumbers are used to identify similar or analogous components orfeatures, but the use of the same reference number does not imply thatthe parts should be construed to be identical. Indeed, in many examplesdescribed herein, the identically numbered parts are distinct instructure and/or function.

Intramedullary Nail Implants and Systems

FIGS. 1A and 3F illustrate one example of an intramedullary nail 109,which may comprise a generally elongate body extending from a first,distal portion or end 110 to a second, proximal portion or end 111. Theelongate body may be in the form of an elongate tubular rod configuredto extend longitudinally within the intramedullary canal of a fracturedbone. The elongate rod may be hollow or may be solid along its length.The elongate body may be substantially straight along a longitudinalaxis of the nail 109 or may comprise one or more curves or bends toconform to the anatomical shape of the intramedullary canal. Thecross-section of the nail 109, taken at a right angle to a centrallongitudinal axis of the intramedullary nail 109, may be circular, oval,elliptical, or of any other suitable cross-dimensional shape. Theproximal portion 111 may have an enlarged diameter or head portionrelative to the distal portion 110 of the nail 109. The enlarged headportion 111 may be sized and configured to be received in the greatertrochanter region of the femur. The intramedullary nail 109 may beconfigured to be positioned in the proximal end of the femur forcephalomedullary fixation. It is envisioned, however, that theintramedullary nail 109 may be configured to be positioned through otherapproaches and locations (e.g., distal end) depending on the bone (e.g.,femur, tibia) and type of fracture.

The distal end 110 may include one or more openings 125 configured toreceive one or more bone anchors, fasteners, or distal fixation devices147 that extend transversely through the distal end 110 of theintramedullary nail 109, and are thereby configured to secure the distalend 110 of the nail 109 within the canal. The distal fixation devices147 may include a bone screw or anchor configured for distal locking ofthe nail 109. The distal fixation device 147 may include traditionalpolyaxial or fixed angle locking bone screws and anchors known in theart.

The proximal end 111 may also include one or more openings 123configured to receive one or more bone anchors or fasteners 119 thatextend transversely through the proximal end 111 of the intramedullarynail 109, and are thereby configured to secure the proximal end 111 ofthe nail 109 within the canal. The proximal fixation devices 119 mayinclude a bone screw or anchor configured for proximal locking of thenail 109. The fixation device 119 may be a calcar screw or anchorconfigured to be aimed at a calcar region of the proximal femur, whichmay constitute the best quality bone in the region. The opening 123 andanchor 119 may be angled, for example, about 100-150°, 110-140°, orabout 120-135° relative to the nail 119 to engage the calcar region ofthe bone. The calcar screw 119 may have an enlarged diameter relative tothe distal screw 147. The proximal fixation device 119 may includetraditional polyaxial or fixed angle calcar screws and anchors known inthe art. The proximal end 111 may also include additional openings 123,for example, for one or more cross-locking devices (e.g., device 205described in more detail below).

The intramedullary nail 109 and anchors 119, 147 may be comprised of anysuitable biocompatible materials. The intramedullary nail 109 andanchors 119, 147 may be comprised of titanium, cobalt chrome,cobalt-chrome-molybdenum, stainless steel, tungsten carbide, carboncomposite, plastic or polymer—such as polyetheretherketone (PEEK),polyethylene, ultra high molecular weight polyethylene (UHMWPE),resorbable polylactic acid (PLA), polyglycolic acid (PGA), combinationsor alloys of such materials, or other appropriate biocompatiblematerials that have sufficient strength to secure and hold bone, whilealso having sufficient biocompatibility to be implanted into a body.

System for Intramedullary Nail Implantation

FIGS. 1A and 1B illustrate perspective and side views, respectively, ofone embodiment of a system 101 for implanting an intramedullary nail109. The system 101 includes an insertion tool 103 that has a couplingportion 105 and a handle portion 107. In some embodiments, the couplingportion 105 and the handle portion 107 can be separate parts that areremovably joined together, while in other embodiments the couplingportion 105 and the handle portion 107 can be different regions of asingle, integrally formed component. The coupling portion 105 releasablyengages or couples to the proximal portion 111 of the nail 109. Forexample, the free end of the coupling portion 105 can be provided with asnap-fit design to temporarily retain a position of the intramedullarynail 109 prior to insertion of a fixation device 119 therethrough.However, those skilled in the art will understand that other couplingmechanisms may be employed.

The handle portion 107 may include one or more openings 127, 129configured to receive one or more guide wires 113, 115. In oneembodiment, the system 101 may include first and second guide wires 113,115 as well as an optional guide sheath 117 through which the fixationdevice 119 may pass (e.g., the fixation device 119 can be inserted usingthe driver 121). As illustrated, the first and second guide wires 113,115 may pass on opposing sides of both the nail 109 and the fixationdevice 119 (e.g. on posterior and anterior sides). Although theillustrated embodiment shows two guide wires, in other embodiments asingle guide wire and corresponding guide wire hole may be used. Instill other embodiments, three or more guide wires may be used.Additionally, the position and orientation of the guide wire holes canvary in different embodiments, for example being disposed moreproximally or more distally along the insertion tool, etc.

As illustrated, the insertion tool 103 allows the user to place one ormore guide wires 113, 115. In one embodiment, the guide wires 113, 155are positioned both anterior and posterior to the nail 109. The guidewires 113, 115 may be positioned in this manner to prevent the distalfragments of the bone (e.g., distal fragments of the femoral head andneck) from rotating about the axis of the fixation device 119 when thefixation device 119 is advanced through the nail 109 and into the boneduring the procedure. The handle portion 107 of the insertion tool 103may include two guide wire receiving features such as holes 127, 129 onthe opposing sides of the tool 103 that allow guide wires 113, 115 topass through the respective holes. The guide wires 113, 115 are passedthrough the soft tissue and into the bone to help stabilize theinsertion tool 103. In this configuration, the insertion tool 103 maynot require any other instruments to guide the wires 113, 115 into thepatient. The insertion tool 103 can achieve stability by resisting bothrotational movement about the axis of the nail 109 as well as axialtranslation along the axis of the nail 109.

FIGS. 2A-2C illustrate various views of the insertion tool 103 of thesystem 101 shown in FIGS. 1A and 1B. In particular, FIG. 2A is apartially exploded perspective view of the insertion tool 103 adjacentto the guide sheath 117, FIG. 2B is a perspective view of the insertiontool 103 with the guide sheath 117 partially inserted therein, and FIG.2C is an enlarged partial cross-sectional view of the engagement betweenthe guide sheath 117 and the insertion tool 103.

The guide sheath 117 can be removably inserted through a guide sheathreceiving feature such as a hole 131 formed in the handle portion 107 ofthe insertion tool 103. The guide sheath hole 131 defines an axis thatintersects with a first aperture 123 in the nail 109. The guide sheath117 can be positioned through the guide sheath hole 131 such that itsubstantially aligns with the first aperture 123 in the nail 109, whichis configured to receive fixation device 119 aimed at the calcar regionof the bone. The guide sheath 117 can include a first retention member133 on an outer surface of the guide sheath 117. The first retentionmember 133 can include, for example, ridged teeth, protrusions, or othersuch surface configured to engage with a corresponding second retentionmember 135 disposed within the guide sheath hole 131. The secondretention member 135 can likewise include one or more ridges orprotrusions. Together the first and second retention members 133, 135form a retention mechanism 137 that allows the guide sheath 117 to beratcheted towards the intramedullary nail 109 while restricting movementof the guide sheath 117 away from the intramedullary nail. The retentionrelease mechanism 139 can disengage the second retention member 135 fromthe first retention member 133 when pressed by a user. For example, theretention release mechanism 139 can be a button disposed on a lowersurface 141 of the handle portion 107. Positioning this retentionrelease mechanism 139 on the lower surface 141 of the insertion handlemay prevent a user from accidentally releasing the guide sheath 117while operating the device (e.g., while grasping the handle portion107).

FIGS. 3A-3F illustrate one method of steps of implanting anintramedullary nail into a fractured femur 143. Referring first to FIG.3A, a proximal end of the femur 143 can be accessed and the medullarycavity of the femur 143 can be reamed using a bone drill and reamer 145.Next, as shown in FIG. 3B, the intramedullary nail 109 is coupled to theinsertion tool 103 and the intramedullary nail 109 is disposed withinthe reamed cavity of the femur 143. In FIG. 3C, when used, one or moreof the first and second guide wires 113 and 115 may be inserted throughthe soft tissue, for example, along parallel trajectories on opposingsides of the nail 109. The guide wires 113, 115 can limit or preventinadvertent rotation of distal fragments of the femur 143 after the nail109 is in position. The proximal fixation device 119 (e.g., a lag screwor other suitable bone anchor) is also passed through the first aperture123 in the nail 109 and into the head/neck region of the femur 143. InFIG. 3D, the guide wires 113, 115 are retracted and in FIG. 3E, thedistal fixation device 147 can additionally be inserted through thedistal aperture 125 in the nail 109. The distal device 147 can bepositioned using the guide sheath 117, which is positioned throughanother opening in the handle portion 107, such that the sheath 1117 isaligned with the distal opening 125 in the nail 109. In FIG. 3F, theinsertion tool 103 is disengaged from the nail 109, which is now securedin place via the proximal fixation device 119 and the distal fixationdevice 147. As shown, the nail 109 may extend along a portion of thelength of femur 143. It is also contemplated, however, that the nail 109may be of different sizes and shapes, for example, of longer lengthsand/or different diameters to accommodate different anatomies andfractures.

Interlocking Fixation Devices for Intramedullary Nail Fixation

FIGS. 4A-4D illustrate another embodiment of an intramedullary nail 201,similar to intramedullary nail 109, with the addition of a cross-lockingfeature for proximal locking of the nail 201. Intramedullary nail 201may include any of the features described above with respect tointramedullary nail 109. Intramedullary nail 201 may further include twointerlocking proximal fixation devices 203, 205 (e.g., bone anchors,fasteners, or screws), for example, by providing converging anddiverging purchase, along with bony fixation in the calcar of the femur229, which is the strongest portion of the hip bone. Accordingly, therisk of failure due to cutout and/or rotation may be reduced.

FIGS. 4A-4D show side, side cross-sectional, and two perspective views,respectively, of the intramedullary nail 201 adjacent to a firstfixation device 203. FIGS. 5A-5D illustrate side, side cross-sectional,and two perspective views, respectively, of the first, proximal fixationdevice 203 inserted through the intramedullary nail 201. FIGS. 6A-6Dillustrate side, side cross-sectional, and two perspective views,respectively, of the system with a second, cross-locking fixation device205 adjacent to the intramedullary nail 201 with the first fixationdevice 203 inserted therein. FIGS. 7A-7D illustrate side, sidecross-sectional, and two perspective views, respectively, of the systemwith the second fixation device 205 inserted through both theintramedullary nail 201 and the first fixation device 203, therebycreating a cross-locking feature for proximal locking of the nail 201.

Referring to FIGS. 4A-8C together, the intramedullary nail 201 isconfigured to receive both the first and second fixation devices 203 and205 therein. The intramedullary nail 201 includes an elongated body 207having first and second apertures 209 and 211 formed therethrough in aproximal region 213, as well as a third aperture 215 formed in a distalregion 217. The first aperture 209 can be sized and configured toreceive the first fixation device 203 therethrough and the secondaperture 211 can be sized and configured to receive the second fixationdevice 205 therethrough.

The first fixation device 203, may be the same or similar to theproximal fixation device 119, described herein, and may include a bonescrew or anchor configured for proximal locking of the nail 201. Forexample, the first fixation device 203 may be a hip screw or anchorconfigured to be aimed at a head region of the proximal femur. Theanchor 203 may have a threaded portion at its distal tip and anon-threaded portion along a substantial length of the screw 203. Theanchor 203 may include traditional polyaxial or fixed angle screws andanchors known in the art.

The second fixation device 205 may also include a bone screw or anchorconfigured for proximal locking of the nail 201. This bone anchor orscrew 205 may be substantially smaller in length and diameter relativeto the calcar screw 203. The bone anchor or screw 205 is substantiallysized and configured to be positioned through second opening 211 in theproximal end of the nail 201 and into a channel 219 in the firstfixation device 203. Thus, the second device 205 is configured tointerlock with the first fixation device 203, for example, for enhancedpurchase and bony fixation to the bone. The second fixation device 205may be positioned to engage at or near the calcar region of bone.Although shown with the second fixation device 205 positioned above thefirst fixation device 203 and angled downwardly into contact with thefirst fixation device 203, it is also envisioned that these relativepositons may be reversed or the fixation devices 203, 205 may otherwisebe angled with respect to one another in order to interlock the devices203, 205 with one another. The second fixation device 205 may beconfigured to pass through a slot or channel 219 formed in the firstfixation device 203. This interlocking feature of the first and secondfixation devices 203, 205 can prevent cutout and rotation by providingconverging and diverging purchase. In the case of a femur, this can alsoprovide bony fixation in the calcar. The elongated slot 219 in the firstfixation device 203 allows for controlled collapse, which leverages thenatural compression between fragments from weight bearing orligamentotaxis. Limited collapse is controlled by the length of the slot219 to prevent the uncontrolled and excessive shortening of the femoralneck. The first fixation device 203 may include distal threads 221 and aproximal drive interface 223 configured to engage with a driver (notshown). The second fixation device 205 may have a narrower diameter thanthe first fixation device 203 such that the second fixation device 205can pass through the slot 219 in the first fixation device 203. Thesecond fixation device 205 may also include distal threads 225 and aproximal drive interface 227 configured to engage with a driver (notshown).

The slot 219 can be disposed in the mid-shaft of the first fixationdevice 203 and may be sized and configured to allow the second fixationdevice 205 to pass therethrough. The slot 219 may be longer thannecessary to allow translation of the first fixation device 203 afterthe second fixation device 205 is in place. The slot 219 may be strongenough to prevent rotation of the first fixation device 203 after thesecond fixation device 205 is in position. The slot 219 may have beveledproximal and distal edges to maximize material in the first fixationdevice 203 while allowing proximal and distal clearance of the secondfixation device 205. The slot 219, in the first fixation device 203, maybe symmetric to allow positioning of the second fixation device 205 in180° increments, for example.

In at least one embodiment, a locking device 230, such as a set screw orwasher, may be used to lock the first and/or the second fixation devices203, 205 into position. As best seen in FIG. 7B, the locking device 230may be threaded through a hollow interior portion of the nail 201. Thelocking device 230 may have external threads, which are sized andconfigured to correspond to mating internal threads along the hollowinterior portion of the nail 201. As the locking device 230 is threadeddownwardly and comes into contact with the first or second fixationdevices 203, 205, the respective fixation device 203, 205 is locked intopositon relative to the nail 201. In some embodiments, the interlockingfixation devices 203, 205 can be used selectively. For example, thethreaded locking device 230 may be threaded to engage the secondfixation device 205; alternatively, the threaded locking device 230 maybe threaded further down to lock the first fixation device 203, forexample, if the second fixation device 205 is not used. This allowsusers the choice of a traditional or interlocking constructintraoperatively.

An insertion tool 103 for implanting the system including the nail 201and the interlocking first and second fixation devices 203 and 205 canbe substantially similar to the system 101 described above with respectto FIGS. 1A-2C, except that an additional guide sheath hole may beformed in the handle portion 107 to accommodate a guide sheath along anappropriate trajectory to insert the second fixation device 205 throughthe second aperture 211 in the nail 201 and into engagement with thefirst fixation device 203.

FIGS. 8A-8C illustrate one method of steps of implanting anintramedullary nail 201 with interlocking fixation devices 203, 205 intoa fractured femur 229. Referring first to FIG. 8A, the nail 201 has beeninserted into a reamed medullary cavity of the femur 229 and the firstfixation device 203 has been inserted through the first aperture 209 inthe nail 201, similar to the technique described above with respect toFIGS. 3A-3D. Referring to FIG. 8B, a distal fixation device 231 can beinserted through the third aperture 215 in the nail 201, similar to thetechnique described above with respect to FIG. 3E. Referring to FIG. 8C,the second fixation device 205 is inserted through the second aperture211 in the nail 201 and through the slot 219 in the first fixationdevice 203. As noted, these intersecting first and second fixationdevices 203, 205 provide additional purchase in the head and neck regionof the femur 229, and in particular the second fixation device 205 canprovide bony fixation in the calcar. Accordingly, the interlocking firstand second fixation devices 203, 205 can provide for improved stabilityand protection against common modes of intramedullary nail implantfailure.

Turning now to FIGS. 9A-12E, cross-locking system 300 is shown accordingto yet another embodiment. This embodiment is similar to thecross-locking embodiment shown in FIGS. 4A-7D except the two crossingslots 219 are replaced with a single elongated slot 319 in the firstfixation device 303. The intramedullary nail 201 and second fixationdevice 205 are the same or similar to those described herein.

With reference to FIGS. 9A-9C, an alternative version of thecross-locking system 300 is shown. The intramedullary nail 201 and thefirst fixation device 303 are depicted in a perspective view, side view,and cross-sectional view, respectively. The first fixation device 303may be in the form of a bone anchor configured for proximal locking ofthe nail 201. For example, the first fixation device 303 may be a hipanchor, for example, configured to be aimed at a neck region of a longbone. The first fixation device 303 may extend from a proximal endhaving a proximal drive feature 323, such as an opening for receiving adriver, to a distal end including a threaded portion 321. A non-threadedportion may extend from the proximal end along a substantial length ofthe anchor 303. The anchor 303 may include features of traditionalpolyaxial or fixed angle screws and anchors known in the art.

The first fixation device 303 includes an elongate opening, slot, orchannel 319 extending therethrough. The channel 319 may be disposed inthe mid-shaft of the first fixation device 303, for example, along thenon-threaded portion. As best seen in FIG. 12E, the elongated slot 319may extend from a proximal end 325 to a distal end 327. The proximal anddistal ends 325, 327 of the elongate slot 319 may be straight, rounded,beveled, angled, or the like. In the embodiment shown, the proximal anddistal ends 325, 327 may each transition from a first angled portion toa curved central portion to a second angled portion.

The second fixation device 205 is configured to interlock with the firstfixation device 303. The second fixation device 205 is sized andconfigured to be positioned through the second opening 211 in theproximal end of the nail 201 and into the channel 319 in the firstfixation device 303. The second fixation device 205 is configured topass through the slot or channel 319 formed in the first fixation device303 to provide for an interlocking feature of the first and secondfixation devices 303, 205. The elongated slot 319 in the first fixationdevice 303 may provide for controlled or limited collapse of the firstand second fixation devices 303, 2015, which may be controlled by thelength of the slot 319.

The second fixation device 205 may be positioned at an angle α relativeto the intramedullary nail 201. The angle α may extend between alongitudinal axis of the intramedullary nail 201 and a longitudinal axisof the second fixation device 205. The angle α may range from about0-130°, about 0-90°, about 70-90°, or about 80-90°. The opening oraperture 211 in the intramedullary nail 201 may be angled, beveled, orprovided with enough clearance to allow for variable angles of angle α.As shown in the side view and cross-sectional views of FIGS. 12A and12B, respectively, second fixation device 205 may be at angle α of lessthan 90°. In FIGS. 12C and 12D, the second fixation device 205 is shownat angle α of about 90°.

The second fixation device 205 is also positioned at an angle β relativeto the first fixation device 303. The angle β may extend between alongitudinal axis of the first fixation device 303 and a longitudinalaxis of the second fixation device 205 relative to their distal mosttips. The angle β may range from about 0-120°, about 0-90°, about 0-65°,about 0-45°, or about 25-65°. The opening or aperture 209 in theintramedullary nail 201 may be angled, beveled, or provided with enoughclearance to allow for variable angles of angle β.

The channel or slot 319 may be sized substantially larger than an outerdiameter of the second fixation device 205, for example, more thandouble, triple, or quadruple the outer diameter of the second fixationdevice 205. The enlarged slot 319 is sized to allow the second fixationdevice 205 to pass therethrough and translate along the length of theslot 319. The elongated slot 319 may allow for translation of the firstfixation device 303 and/or the second fixation device 205 after thefirst and second fixation devices 303, 205 are implanted in bone. Afterimplantation, the second fixation device 205 may reside within the slot319 without contacting either of the proximal or distal ends 325, 327.The second fixation device 205 may be permitted to translate in the slot319 until the second fixation device 205 contacts one of the firstproximal or distal ends 325, 327, for example, one of the angledportions of the end 325, 327.

The cross-locking system 300 may address one or more of the majorfailure modes for hip fixation: axial cutout, cephalad cutout, fragmentrotation, and nonunion. For example, the intersecting first and secondfixation devices 303, 205 may provide for enhanced purchase in the headand neck region of the elongate bone. The overall system 300 can providefor improved stability and protection against common modes of implantfailure.

CONCLUSION

The above detailed descriptions of embodiments of the technology are notintended to be exhaustive or to limit the technology to the precise formdisclosed above. Although specific embodiments of, and examples for, thetechnology are described above for illustrative purposes, variousequivalent modifications are possible within the scope of thetechnology, as those skilled in the relevant art will recognize. Forexample, while steps are presented in a given order, alternativeembodiments may perform steps in a different order. The variousembodiments described herein may also be combined to provide furtherembodiments.

From the foregoing, it will be appreciated that specific embodiments ofthe invention have been described herein for purposes of illustration,but well-known structures and functions have not been shown or describedin detail to avoid unnecessarily obscuring the description of theembodiments of the technology. Where the context permits, singular orplural terms may also include the plural or singular term, respectively.

Moreover, unless the word “or” is expressly limited to mean only asingle item exclusive from the other items in reference to a list of twoor more items, then the use of “or” in such a list is to be interpretedas including (a) any single item in the list, (b) all of the items inthe list, or (c) any combination of the items in the list. Additionally,the term “comprising” is used throughout to mean including at least therecited feature(s) such that any greater number of the same featureand/or additional types of other features are not precluded. It willalso be appreciated that specific embodiments have been described hereinfor purposes of illustration, but that various modifications may be madewithout deviating from the technology. Further, while advantagesassociated with certain embodiments of the technology have beendescribed in the context of those embodiments, other embodiments mayalso exhibit such advantages, and not all embodiments need necessarilyexhibit such advantages to fall within the scope of the technology.Accordingly, the disclosure and associated technology can encompassother embodiments not expressly shown or described herein.

What is claimed is:
 1. An implant, comprising: an intramedullary nailhaving: an elongate body extending from a proximal portion to a distalportion, a portion of the elongate body extending along a first axis; afirst aperture formed in the proximal portion, the first aperturedefining a second axis transverse to the first axis; and a secondaperture formed in the proximal portion, the second aperture beingspaced apart from the first aperture, the second aperture defining athird axis transverse to the first axis, the third axis intersectingwith the second axis at a point spaced apart from the body; a firstfixation device positionable through the first aperture in the nail, thefirst fixation device having an elongate slot; and a second fixationdevice positionable through the second aperture in the nail, and thesecond fixation device positionable through the elongate slot in thefirst fixation device.
 2. The implant of claim 1, wherein the firstfixation device extends from a proximal end portion to a distal endportion, and the first fixation device has a threaded distal portion. 3.The implant of claim 2, wherein the elongate slot is positionedcentrally between the distal end portion and the proximal end portion.4. The implant of claim 1, wherein the second fixation device isthreaded along its length.
 5. The implant of claim 1, wherein theelongate slot in the first fixation device is sized to allow translationof the first fixation device after the second fixation device has beenpassed through the slot.
 6. The implant of claim 1, wherein an anglebetween the first and second fixation devices is up to 120° betweendistal tips of the first and second fixation devices.
 7. The implant ofclaim 1, wherein the elongate slot in the first fixation devicecomprises beveled proximal and distal edges.
 8. The implant of claim 1,wherein the intramedullary nail further comprises a third aperture inthe distal portion of the nail.
 9. The implant of claim 7, wherein athird fixation device is positionable through the third aperture tothereby secure the distal portion of the nail.
 10. An implantcomprising: an intramedullary nail having: an elongate body having afirst axis and extending from a proximal portion to a distal portion; afirst aperture formed in the proximal portion, the first aperturedefining a second axis transverse to the first axis; and a bone anchorhaving an elongate slot positioned centrally therethrough, the boneanchor positionable through the first aperture in the nail such that theelongate slot is positioned outside the intramedullary nail.
 11. Theimplant of claim 10, wherein the intramedullary nail further comprises asecond aperture formed in the proximal portion, the second aperturebeing spaced apart from the first aperture.
 12. The implant of claim 11,wherein the second aperture defines a third axis transverse to the firstaxis, the third axis intersects with the second axis at a point spacedapart from the elongate body.
 13. The implant of claim 11, furthercomprising a calcar screw positionable through the second aperture inthe nail.
 14. The implant of claim 13, wherein the calcar screw ispositioned through the elongate slot in the bone anchor.
 15. The implantof claim 13, wherein the calcar screw is threaded along its length. 16.The implant of claim 13, wherein the elongate slot in the bone anchor issized to allow translation of the bone anchor and calcar screw after thecalcar screw has been passed through the slot.
 17. The implant of claim10, wherein the elongate slot comprises beveled proximal and distaledges.
 18. The implant of claim 10, further comprising a third aperturein the distal portion of the nail.
 19. The implant of claim 19, whereina distal fixation device is positionable through the third aperture fordistal locking of the intramedullary nail.